G38D (p.Gly38Asp) variant of ABCC2 (Q92887)
G38D (p.Gly38Asp) in ABCC2 (Q92887) is a missense change. The record also includes structural context.
G38D (p.Gly38Asp) variant details
- p.Gly38Asp
- Ensembl rs2037675235
- Missense
- Structural context available